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dc.contributor.authorKnapp, Thomas G
dc.contributor.authorDuan, Suzann
dc.contributor.authorMerchant, Juanita L
dc.contributor.authorSawyer, Travis W
dc.date.accessioned2023-01-09T23:23:31Z
dc.date.available2023-01-09T23:23:31Z
dc.date.issued2022-12-14
dc.identifier.citationKnapp, T. G., Duan, S., Merchant, J. L., & Sawyer, T. W. (2022). Quantitative characterization of duodenal gastrinoma autofluorescence using multiphoton microscopy. Lasers in Surgery and Medicine.en_US
dc.identifier.pmid36515355
dc.identifier.doi10.1002/lsm.23619
dc.identifier.urihttp://hdl.handle.net/10150/667377
dc.description.abstractBackground: Duodenal gastrinomas (DGASTs) are neuroendocrine tumors that develop in the submucosa of the duodenum and produce the hormone gastrin. Surgical resection of DGASTs is complicated by the small size of these tumors and the tendency for them to develop diffusely in the duodenum. Endoscopic mucosal resection of DGASTs is an increasingly popular method for treating this disease due to its low complication rate but suffers from poor rates of pathologically negative margins. Multiphoton microscopy can capture high-resolution images of biological tissue with contrast generated from endogenous fluorescence (autofluorescence [AF]) through two-photon excited fluorescence (2PEF). Second harmonic generation is another popular method of generating image contrast with multiphoton microscopy (MPM) and is a light-scattering phenomenon that occurs predominantly from structures such as collagen in biological samples. Some molecules that contribute to AF change in abundance from processes related to the cancer disease process (e.g., metabolic changes, oxidative stress, and angiogenesis). Study Design/Materials and Methods: MPM was used to image 12 separate patient samples of formalin-fixed and paraffin-embedded duodenal gastrinoma slides with a second-harmonic generation (SHG) channel and four 2PEF channels. The excitation and emission profiles of each 2PEF channel were tuned to capture signal dominated by distinct fluorophores with well-characterized fluorescent spectra and known connections to the physiologic changes that arise in cancerous tissue. Results: We found that there was a significant difference in the relative abundance of signal generated in the 2PEF channels for regions of DGASTs in comparison to the neighboring tissues of the duodenum. Data generated from texture feature extraction of the MPM images were used in linear discriminant analysis models to create classifiers for tumor versus all other tissue types before and after principal component analysis (PCA). PCA improved the classifier accuracy and reduced the number of features required to achieve maximum accuracy. The linear discriminant classifier after PCA distinguished between tumor and other tissue types with an accuracy of 90.6%−93.8%. Conclusions: These results suggest that multiphoton microscopy 2PEF and SHG imaging is a promising label-free method for discriminating between DGASTs and normal duodenal tissue which has implications for future applications of in vivo assessment of resection margins with endoscopic MPM.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.rights© 2022 Wiley Periodicals LLC.en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en_US
dc.subjectGEP-NETen_US
dc.subjectadvanced microscopyen_US
dc.subjectduodenal gastrinomaen_US
dc.subjectMultiphoton Microscopyen_US
dc.subjectneuroendocrine tumoren_US
dc.subjectoptical diagnosticsen_US
dc.subjectquantitative microscopyen_US
dc.subjectsecondharmonic generationen_US
dc.subjecttissue classificationen_US
dc.subjecttwo-photon excited fluorescenceen_US
dc.titleQuantitative characterization of duodenal gastrinoma autofluorescence using multiphoton microscopyen_US
dc.typeArticleen_US
dc.identifier.eissn1096-9101
dc.contributor.departmentDepartment of Biomedical Engineering, University of Arizonaen_US
dc.contributor.departmentCollege of Medicine, University of Arizonaen_US
dc.contributor.departmentWyant College of Optical Sciences, University of Arizonaen_US
dc.identifier.journalLasers in surgery and medicineen_US
dc.description.note12 month embargo; first published: 14 December 2022en_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal accepted manuscripten_US
dc.source.journaltitleLasers in surgery and medicine
dc.source.countryUnited States


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